FDA 510(k)

COMPLETE CONTROL 系统Gen2

K号: K191083 · 2019-05-24

决定日期2019-05-24

产品代码GXY

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决定实质等同

器械摘要

COMPLETE CONTROL System Gen2 is the device name listed in this FDA 510(k) record. The listed applicant is Coapt, LLC. It received FDA 510(k) clearance on 2019-05-24 under 510(k) number K191083. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the COMPLETE CONTROL System Gen2?

COMPLETE CONTROL System Gen2 is a medical device that received FDA 510(k) clearance on 2019-05-24. The listed applicant is Coapt, LLC. The 510(k) number is K191083.

When did COMPLETE CONTROL System Gen2 receive FDA 510(k) clearance?

COMPLETE CONTROL System Gen2 received FDA 510(k) clearance on 2019-05-24, under 510(k) number K191083.

Who is the listed applicant for COMPLETE CONTROL System Gen2?

The FDA 510(k) record lists Coapt, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPLETE CONTROL System Gen2?

The FDA product code for COMPLETE CONTROL System Gen2 is GXY.

列明Coapt, LLC为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K190416Dome 电极 K162891Complete Control System

相关器械（代码：GXY）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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